HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 22768412, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Chloro-2-hydrazinyl-5-phenyl-3H-1,4-benzodiazepine | HCID 12390874 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22768412 | HCID 22768412 | — |
Reaction Steps
To a solution of 1.4 parts of 7-chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine, prepared in Example 1, in 25 parts by volume of tetrahydrofuran is added 0.62 part by volume of benzoyl chloride, and the mixture is stirred at room temperature for 2 hours to complete the reaction. The reaction mixture is neutralized with a saturated aqueous solution of sodium bicarbonate. The resulting white precipitate is separated, washed with water and then with methanol, and dried, whereby 2-(2-benzoylhydrazino)-7-chloro-5-phenyl-3H-1,4-benzodiazepine is yielded as crystals. Recrystallization from a mixture of chloroform and methanol yields white needles melting at 207° C to 208° C (effervescence).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04116956 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-c06c7db227304bc590742438d1764b2a |
| Source note | uspto-grants-1978_09 |